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2- propanol dehydration

Isobutyl alcohol, isobutanol, 2-methyl-propanol, isopropyl carbinol, Me2CHCH20H. B.p. 108°C. Occurs in fusel-oil. Oxidized by potassium permanganate to 2-methyl-propanoic acid dehydrated by strong sulphuric acid to 2-methylpropene. [Pg.71]

In the acid catalyzed dehydration of 2 methyl 1 propanol what carbocation would be formed if a hydride shift accompanied cleavage of the carbon-oxygen bond in the alkyloxonium lon" What ion would be formed as a result of a methyl shift" Which pathway do you think will predominate a hydnde shift or a methyl shift" ... [Pg.228]

Membranes and Osmosis. Membranes based on PEI can be used for the dehydration of organic solvents such as 2-propanol, methyl ethyl ketone, and toluene (451), and for concentrating seawater (452—454). On exposure to ultrasound waves, aqueous PEI salt solutions and brominated poly(2,6-dimethylphenylene oxide) form stable emulsions from which it is possible to cast membranes in which submicrometer capsules of the salt solution ate embedded (455). The rate of release of the salt solution can be altered by surface—active substances. In membranes, PEI can act as a proton source in the generation of a photocurrent (456). The formation of a PEI coating on ion-exchange membranes modifies the transport properties and results in permanent selectivity of the membrane (457). The electrochemical testing of salts (458) is another possible appHcation of PEI. [Pg.14]

Although most of the installed solvent dehydration systems have been for ethanol dehydration, dehydration of other solvents including 2-propanol, ethylene glycol, acetone, and methylene chloride, has been considered. [Pg.87]

Fig. 5. 2-Propanol dehydration where A2eo is a2eotrope, (-) are tie lines, and the shaded areas represent the region of two Hquid phases. Initial... Fig. 5. 2-Propanol dehydration where A2eo is a2eotrope, (-) are tie lines, and the shaded areas represent the region of two Hquid phases. Initial...
A structurally unrelated agent is tazadolene (40). The synthesis of tazadolene begins with P-keto ester 37 and subsequent enamine formation with 3-amino-1-propanol followed by hydrogenolysis to give 38. This phenylhydroxymethyl compound is then dehydrated with hydrochloride acid to form olefin 39. Treatment with bromine and triphenylphosphine effects cycliza-tion to form the azetidine ring of tazadolene [10]. [Pg.6]

Nitrn-l-propene Preparation is accomphshed by dehydration of l-nitro-2-propanol with methanesuLfonyl chloride and triethylamine (30% ieldi, acetic... [Pg.39]

Problem 18.2 Why do you suppose only symmetrical ethers are prepared by the sulfuric add-catalyzed dehydration procedure What product(s) would you expect if ethanol and 1-propanol were allowed to react together In what ratio would the products be formed if the two alcohols were of equal reactivity ... [Pg.656]

The water-insoluble salts such as Cs2,5Ho., iPWi204o efficiently catalyse dehydration of 2-propanol in the gas phase and alkylation of m-xylene and trimethyl benzene with cyclohexene this catalyst is much more active than Nafion-H, HY-zeolite, H-ZSM-5, and sulphated zirconia (Okuhara et al., 1992). [Pg.138]

Friedel-Crafts alkylation can occur intramolecularly to form a fused ring. Intramolecular Friedel-Crafts reactions provide an important method for constructing polycyclic hydrocarbon frameworks. It is somewhat easier to form six-membered than five-membered rings in such reactions. Thus, whereas 4-phenyl-1-butanol gives a 50% yield of a cyclized product in phosphoric acid, 3-phenyl-1-propanol is mainly dehydrated to alkenes.43... [Pg.1016]

Because G and H are state functions, changes in these quantities are independent of whether the reaction takes place in one or in several steps. Consequently, it is possible to tabulate data for relatively few reactions and use this data in the calculation of AG° and AH0 for other reactions. In particular, one tabulates data for the standard reactions that involve the formation of a compound from its elements. One may then consider a reaction involving several compounds as being an appropriate algebraic sum of a number of elementary reactions, each of which involves the formation of one compound. The dehydration of n-propanol... [Pg.7]

Nitro-l-propene Preparation is accomplished by dehydration of 2-nitro-l-propanol with phthalic anhydride (73%)45 or acetic anhydride-AcONa46 bp 56-57 °C/80 mmHg. [Pg.39]

Izumi and Urabe [105] found first that POM compounds could be entrapped strongly on active carbons. The supported POMs catalyzed etherization of ferf-butanol and n-butanol, esterification of acetic acid with ethanol, alkylation of benzene, and dehydration of 2-propanol [105], In 1991, Neumann and Levin [108] reported the oxidation of benzylic alcohols and amines catalyzed by the neutral salt of Na5[PV2Mo10O40] impregnated on active carbon. Benzyl alcohols were oxidized efficiently to the corresponding benzaldehydes without overoxidation ... [Pg.475]

Table 2. The characteristics of the iso-propanol (IPA) dehydration process, by using pervaporation technique, through (PAA.HCl)-PVA membrane... Table 2. The characteristics of the iso-propanol (IPA) dehydration process, by using pervaporation technique, through (PAA.HCl)-PVA membrane...
A palladium phosphine complex [e.g., BCPE = l,2-bis(l,5-cyclooctylenephos-phino)ethane] was also reported to produce propanediols and n-propanol from glycerol at 443 K under 6 MPa CO/H2 atmosphere in acidic conditions, n-Propanol is the dominant product, while a slight preference for the formation of propane-1,3-diol is seen in the diol fraction. Reactions were performed at different temperatures in the range 413-448 K. Since acrolein was monitored at high temperature, a reaction network was proposed following a sequential dehydration/hydrogenation pathway [20]. [Pg.249]

Melhyl-l-propanol Isobutyl Alcohol) and 2-Phenyl-1-propanol Herling and Pines (SO) studied the dehydration of 2-methyl-l-propanol and 2-phenyl-1-propanol. The two alcohols were passed over alumina under nonacidic conditions at temperatures of 350° and 270°, respectively (Tables III and IV). The 2-methyl-l-propanol underwent, in part, skeletal isomerization forming butenes, whereby the ratio of cisjtrans 2-butene produced was four to six times greater than the equilibrium ratio. The extent of skeletal isomerization depended to some extent on the method of preparation of the alumina. [Pg.75]

Dehydration of 2-Methyl-1-propanol over Alumina Catalysts at 350°... [Pg.75]


See other pages where 2- propanol dehydration is mentioned: [Pg.295]    [Pg.373]    [Pg.491]    [Pg.455]    [Pg.267]    [Pg.394]    [Pg.373]    [Pg.298]    [Pg.485]    [Pg.361]    [Pg.361]    [Pg.451]    [Pg.241]    [Pg.243]    [Pg.765]    [Pg.125]    [Pg.127]    [Pg.244]    [Pg.407]    [Pg.173]    [Pg.183]    [Pg.77]   
See also in sourсe #XX -- [ Pg.360 ]




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2 Methyl 2 propanol acid catalyzed dehydration

2-Phenyl-1-propanol dehydration

Dehydration of 2-Propanol to Propene

Dehydration of 2-propanol

Elimination 2-propanol dehydration

Propanol 2-methyl-, dehydration

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